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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249155Generated: October 29, 2026

Hydrochloric Acid → Benzyl 4-[3-(3-nitrobenzyl)indol-1-yl]-4-oxobutyrate

https://huagongshe.com/reaction/249155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant3-(3-Nitrobenzyl)indoleHCID 19024704—
ReactantBenzyl phenyl succinateHCID 19024784—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-[3-(3-nitrobenzyl)indol-1-yl]-4-oxobutyrateHCID 1902472974.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3-(3-nitrobenzyl)indole (280 mg) in N,N-dimethylformamide (5 ml) was added to a suspension of sodium hydride (60% dispersion in mineral oil, 66.6 mg) in N,N-dimethylformamide (10 ml) at 0° C. The mixture was stirred at 25° C. for 40 minutes, and a solution of benzyl phenyl succinate (316 mg) in N,N-dimethylformamide was added at -40° C. After stirred at -40° C. for 20 minutes, the reaction mixture was poured into a mixture of ethyl acetate and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, and dried over, magnesium sulfate. After evaporation of the solvent, the crude crystals were washed with hot isopropyl ether to give benzyl 4-[3-(3-nitrobenzyl)indol-1-yl]-4-oxobutyrate (364 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-f987f97db3f54769b1057ea5e79dfa11
Source noteuspto-grants-1993_05